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U.S. Department of Health and Human Services

Class 2 Device Recall Contour VL Ureteral Stent

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 Class 2 Device Recall Contour VL Ureteral Stentsee related information
Date Initiated by FirmNovember 16, 2020
Create DateDecember 30, 2020
Recall Status1 Open3, Classified
Recall NumberZ-0757-2021
Recall Event ID 86880
510(K)NumberK974541 
Product Classification Stent, ureteral - Product Code FAD
ProductContour VL Variable Length Ureteral Stent, UPN M0061801550, M0061801560, M0061801570
Code Information GTIN 08714729058410:  Lots  25578577, 25598812, 25609220, 25614542, 25614545, 25619687, 25641771, 25713852, 25753933, 25790349.   GTIN 08714729067986:  Lots  25640715, 25670518, 25686790, 25686791, 25686792, 25741763, 25741770, 25753937, 25790351, 25795704, 25802759, 25809481, 25822104.   GTIN 08714729068020:  Lots  25578740, 25583824.
FEI Number 3005099803
Recalling Firm/
Manufacturer		 Boston Scientific Corporation
300 Boston Scientific Way
Marlborough MA 01752-1291
For Additional Information ContactNicole Pshon
763-494-1133
Manufacturer Reason
for Recall		Trace amounts of metallic debris were found on the stent related to the manufacturing process. The debris was confirmed to be particles of nickel.
FDA Determined
Cause 2		Process design
ActionOn November 16, 2020, the firm distributed Urgent Medical Device Removal letters to affected customers. Customers were informed of the product issue and asked to take the following actions: - Verify whether you have any product from the affected lots/batches within your inventory - Immediately cease use or distribution of any remaining unused product from the affected lots/batches - Segregate affected material and return it to BSC in accordance with removal instructions included in the letter. - Distributors should forward the notification to their customers Your local Sales Representative can answer any questions that you may have regarding this notification.
Quantity in Commerce458 units
DistributionDistribution US nationwide and Japan.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = FAD
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